HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1279028Generated: November 1, 2026
Dimethylcarbamoyl Chloride → n,n-Dimethylpiperazine-1-carboxamide
https://huagongshe.com/reaction/1279028
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylcarbamoyl Chloride | HCID 6598 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | n,n-Dimethylpiperazine-1-carboxamide | HCID 712909 | — |
Reaction Steps
To a solution of 1.92 g 1-(1,1-dimethylethyloxycarbonyl)piperazine in 11 mL of dichloromethane and 1.5 mL of triethylamine at room temperature was added dropwise 1 mL of dimethylcarbamylchloride. After 16 hours 5% aqueous sodium hydrogencarbonate and dichloromethane were added, the organic layer separated, dried over magnesium sulfate and concentrated. Column chromatography on silica gel (dichloromethane/methanol=95/5 v/v) yielded 1.34 g 1-1,1-dimethylethyloxycarbonyl)-4-(dimethylaminocarbonyl)piperazine. This compound was dissolved in a 3N hydrogen chloride solution in methanol at 0° C. After 15 min the reaction mixture was allowed to warm to room temperature and After stirring for 3 days at room temperature the reaction mixture was concentrated to give 1.06 g of 1-(dimethylaminocarbonyl)piperazine hydrochloride. rf=0.29, SiO2: dichloromethane/methanol=4/1 v/v.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06444672B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-b08e3076c53c4e67b32782100ecd448b |
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| Source note | uspto-grants-2002_09 |
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